首页> 外文期刊>The Journal of dermatological treatment >A randomized study comparing the combination of nbUVB and etanercept to etanercept monotherapy in patients with psoriasis who do not exhibit an excellent response after 12 weeks of etanercept
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A randomized study comparing the combination of nbUVB and etanercept to etanercept monotherapy in patients with psoriasis who do not exhibit an excellent response after 12 weeks of etanercept

机译:一项随机研究比较了nbUVB和依那西普联合依那西普单药治疗在牛皮癣患者中接受依那西普12周后无良好反应的银屑病患者

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Background: There is a lack of data on the combination of phototherapy with etanercept in patients who have not shown an excellent response to etanercept monotherapy. Objectives: To study the combination of narrow-band ultraviolet B (nbUVB) phototherapy with etanercept in patients not demonstrating an improvement of 90% in their Psoriasis Area Severity Index (PASI-90) after 12 weeks of etanercept. Patients and methods: Psoriatic patients not reaching PASI-90 after 12 weeks of etanercept therapy were randomized (1:1) to receive either etanercept (50 mg once a week) monotherapy or in combination with nbUVB three times weekly for periods of 4 weeks. Results: Seventy-five patients were randomized. Only 21.6% of patients achieved adherence of 80% or more for nbUVB treatments. At week 24, PASI-90 was reached by 16.2% of patients in the etanercept plus nbUVB group when compared with 15.8% of patients in the etanercept monotherapy group (p = 1.000). In patients with high adherence to nbUVB, the PASI-90 at week 16 was 42.9% for etanercept with nbUVB when compared with 3.4% for etanercept monotherapy (p = 0.018). Both treatments were well tolerated. Conclusion: Addition of nbUVB after 12 weeks of etanercept did not significantly improve the clinical response except for a subset of patients with high adherence to nbUVB.Clinical Trials Registration number: NCT00640393.
机译:背景:对于依那西普单药治疗无明显疗效的患者,缺乏光疗与依那西普联用的数据。目的:研究窄带紫外线B(nbUVB)光疗与依那西普联用的患者,在依那西普治疗12周后银屑病面积严重性指数(PASI-90)并未改善90%。患者和方法:将依那西普治疗12周后未达到PASI-90的银屑病患者随机(1:1)接受伊那西普(每周一次50 mg)单一疗法或与nbUVB组合,每周3次,共4周。结果:75例患者被随机分组​​。只有21.6%的患者通过nbUVB治疗达到了80%或更高的依从性。在第24周时,依那西普联合nbUVB组的患者中PASI-90达到了16.2%,而依那西普单药治疗组中则为15.8%(p = 1.000)。在对nbUVB依从性较高的患者中,依那西普与nbUVB在16周时的PASI-90为42.9%,而依那西普单一疗法为3.4%(p = 0.018)。两种治疗均耐受良好。结论:依那西普12周后添加nbUVB并不能显着改善临床反应,除了一部分对nbUVB依从性高的患者。临床试验注册号:NCT00640393。

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